Mechanisms of environmental chemicals that enable the cancer hallmark of evasion of growth suppression

. 2015 Jun ; 36 Suppl 1 (Suppl 1) : S2-18.

Jazyk angličtina Země Velká Británie, Anglie Médium print

Typ dokumentu časopisecké články, Research Support, N.I.H., Extramural, práce podpořená grantem, přehledy

Perzistentní odkaz   https://www.medvik.cz/link/pmid26106139

Grantová podpora
R01 CA113447 NCI NIH HHS - United States
R01 CA192613 NCI NIH HHS - United States
R01 CA92306-S1 NCI NIH HHS - United States
R01 CA157754 NCI NIH HHS - United States
T32 CA009686 NCI NIH HHS - United States
R01 CA92306 NCI NIH HHS - United States
R01 CA092306 NCI NIH HHS - United States
R01CA172392 NCI NIH HHS - United States
R13 ES023276 NIEHS NIH HHS - United States

As part of the Halifax Project, this review brings attention to the potential effects of environmental chemicals on important molecular and cellular regulators of the cancer hallmark of evading growth suppression. Specifically, we review the mechanisms by which cancer cells escape the growth-inhibitory signals of p53, retinoblastoma protein, transforming growth factor-beta, gap junctions and contact inhibition. We discuss the effects of selected environmental chemicals on these mechanisms of growth inhibition and cross-reference the effects of these chemicals in other classical cancer hallmarks.

Advanced Molecular Science Research Centre King George's Medical University Lucknow UP 226003 India

Center for Environmental Carcinogenesis and Risk Assessment Environmental Protection and Health Prevention Agency Bologna 40126 Italy

Center for Genomic Science of Istituto Italiano di Tecnologia Milan 16163 Italy and

Center for Radiological Research Columbia University Medical Center New York NY 10032 USA Instituto de Alta Investigacion Universidad de Tarapaca Arica 8097877 Chile

Department of Anatomy and Cell Biology University of Western Ontario London Ontario N6A 5C1 Canada

Department of Biochemistry and Molecular Biology Dalhousie University Halifax Nova Scotia B3H 4R2 Canada

Department of Biological Chemical and Pharmaceutical Sciences and Technologies Polyclinic Plexus University of Palermo 90127 Palermo Italy

Department of Biological Chemical and Pharmaceutical Sciences and Technologies Polyclinic Plexus University of Palermo 90127 Palermo Italy Sbarro Institute for Cancer Research and Molecular Medicine College of Science and Technology Temple University Philadelphia PA 19122 USA

Department of Biomedical Science Faculty of Medicine and Health Sciences University Putra Serdang Selangor 43400 Malaysia

Department of Cellular and Physiological Sciences Life Sciences Institute Faculty of Medicine The University of British Columbia Vancouver British Columbia V6T 1Z3 Canada

Department of Cytokinetics Institute of Biophysics AS CR Brno 612 65 Czech Republic

Department of Environmental and Radiological Health Sciences Colorado State University Colorado School of Public Health Fort Collins CO 80523 1680 USA

Department of Experimental and Clinical Medicine University of Firenze 50134 Florence Italy

Department of Medicine Medical Oncology Rutgers Cancer Institute of New Jersey New Brunswick NJ 08901 1914 USA

Department of Natural Science The City University of New York at Hostos Campus Bronx NY 10451 USA

Department of Pathology Kuwait University Safat 13110 Kuwait

Department of Pharmacology and Toxicology Ernest Mario School of Pharmacy Rutgers the State University of New Jersey Piscataway NJ 60503 USA

Departments of Neurosurgery and Biochemistry and Massey Cancer Center Virginia Commonwealth University Richmond VA 980033 USA

Departments of Pharmacology and Hematology and Medical Oncology Emory University School of Medicine and Winship Cancer Institute Atlanta GA 30322 USA Department of Pathology Kuwait University Safat 13110 Kuwait Department of Experimental and Clinical Medicine University of Firenze 50134 Florence Italy Department of Biochemistry and Molecular Biology Dalhousie University Halifax Nova Scotia B3H 4R2 Canada Program in Genetics and Molecular Biology Graduate Division of Biological and Biomedical Sciences Emory University Atlanta GA 30322 USA Department of Environmental and Radiological Health Sciences Colorado State University Colorado School of Public Health Fort Collins CO 80523 1680 USA Center for Radiological Research Columbia University Medical Center New York NY 10032 USA Instituto de Alta Investigacion Universidad de Tarapaca Arica 8097877 Chile Division of Hematology and Oncology Department of Pediatrics Children's Healthcare of Atlanta and Emory University Atlanta GA 30322 USA Department of Medicine Medical Oncology Rutgers Cancer Institute of New Jersey New Brunswick NJ 08901 1914 USA Center for Environmental Carcinogenesis and Risk Assessment Environmental Protection and Health Prevention Agency Bologna 40126 Italy Departments of Neurosurgery and Biochemistry and Massey Cancer Center Virginia Commonwealth University Richmond VA 980033 USA Department of Biological Chemical and Pharmaceutical Sciences and Technologies Polyclinic Plexus University of Palermo 90127 Palermo Italy Mediterranean Institute of Oncology 95029 Viagrande Italy Graduate School of Biomedical Sciences and Department of Molecular Biology School of Osteopathic Medicine Rowan University Stratford NJ 08084 1501 USA Department of Biomedical Science Faculty of Medicine and Health Sciences University Putra Serdang Selangor 43400 Malaysia Department of Anatomy and Cell Biology University of Western Ontario London Ontari

Division of Hematology and Oncology Department of Pediatrics Children's Healthcare of Atlanta and Emory University Atlanta GA 30322 USA

Environmental and Molecular Toxicology Environmental Health Sciences Center Oregon State University Corvallis OR 97331 USA

Graduate School of Biomedical Sciences and Department of Molecular Biology School of Osteopathic Medicine Rowan University Stratford NJ 08084 1501 USA

Institute of Molecular Genetics National Research Council 27100 Pavia Italy

Instituto de Alta Investigacion Universidad de Tarapaca Arica 8097877 Chile

Mediterranean Institute of Oncology 95029 Viagrande Italy

Molecular Oncology Program Lombardi Comprehensive Cancer Center Georgetown University Medical Center Washington DC 20057 USA

Program in Genetics and Molecular Biology Graduate Division of Biological and Biomedical Sciences Emory University Atlanta GA 30322 USA

Toxicology Research Division Bureau of Chemical Safety Food Directorate Health Products and Food Branch Health Canada Ottawa Ontario K1A0K9 Canada

Urology Dept kasr Al Ainy School of Medicine Cairo University El Manial Cairo 12515 Egypt

Zobrazit více v PubMed

Lee W., et al. (1994) Solution structure of the tetrameric minimum transforming domain of p53. Nat. Struct. Biol., 1, 877–890. PubMed

Bieging K.T., et al. (2012) Deconstructing p53 transcriptional networks in tumor suppression. Trends Cell Biol., 22, 97–106. PubMed PMC

Goh A.M., et al. (2011) The role of mutant p53 in human cancer. J. Pathol., 223, 116–126. PubMed

Kussie P.H., et al. (1996) Structure of the MDM2 oncoprotein bound to the p53 tumor suppressor transactivation domain. Science, 274, 948–953. PubMed

Popowicz G.M., et al. (2008) Structure of the human Mdmx protein bound to the p53 tumor suppressor transactivation domain. Cell Cycle, 7, 2441–2443. PubMed

Pant V., et al. (2011) Heterodimerization of Mdm2 and Mdm4 is critical for regulating p53 activity during embryogenesis but dispensable for p53 and Mdm2 stability. Proc. Natl. Acad. Sci. USA, 108, 11995–12000. PubMed PMC

Huang L., et al. (2011) The p53 inhibitors MDM2/MDMX complex is required for control of p53 activity in vivo . Proc. Natl. Acad. Sci. USA, 108, 12001–12006. PubMed PMC

Gu J., et al. (2002) Mutual dependence of MDM2 and MDMX in their functional inactivation of p53. J. Biol. Chem., 277, 19251–19254. PubMed

Ray-Coquard I., et al. (2012) Effect of the MDM2 antagonist RG7112 on the P53 pathway in patients with MDM2-amplified, well-differentiated or dedifferentiated liposarcoma: an exploratory proof-of-mechanism study. Lancet Oncol., 13, 1133–1140. PubMed

Wade M., et al. (2013) MDM2, MDMX and p53 in oncogenesis and cancer therapy. Nat. Rev. Cancer, 13, 83–96. PubMed PMC

Smith J., et al. (2010) The ATM-Chk2 and ATR-Chk1 pathways in DNA damage signaling and cancer. Adv. Cancer Res., 108, 73–112. PubMed

Bartek J., et al. (2003) Chk1 and Chk2 kinases in checkpoint control and cancer. Cancer Cell, 3, 421–429. PubMed

Jin J., et al. (2008) Differential roles for checkpoint kinases in DNA damage-dependent degradation of the Cdc25A protein phosphatase. J. Biol. Chem., 283, 19322–19328. PubMed PMC

Zhou B.B., et al. (2003) Targeting DNA checkpoint kinases in cancer therapy. Cancer Biol. Ther., 2(4 Suppl 1), S16–S22. PubMed

Yadavilli S., et al. (2009) Mechanism of diepoxybutane-induced p53 regulation in human cells. J. Biochem. Mol. Toxicol., 23, 373–386. PubMed

Giardiello F.M., et al. (1987) Increased risk of cancer in the Peutz-Jeghers syndrome. N. Engl. J. Med., 316, 1511–1514. PubMed

Avizienyte E., et al. (1999) LKB1 somatic mutations in sporadic tumors. Am. J. Pathol., 154, 677–681. PubMed PMC

Chen R.W., et al. (1999) PTEN and LKB1 genes in laryngeal tumours. J. Med. Genet., 36, 943–944. PubMed PMC

Guldberg P., et al. (1999) Somatic mutation of the Peutz-Jeghers syndrome gene, LKB1/STK11, in malignant melanoma. Oncogene, 18, 1777–1780. PubMed

Zeng P.Y., et al. (2006) LKB1 is recruited to the p21/WAF1 promoter by p53 to mediate transcriptional activation. Cancer Res., 66, 10701–10708. PubMed

Scott K.D., et al. (2007) LKB1 catalytically deficient mutants enhance cyclin D1 expression. Cancer Res., 67, 5622–5627. PubMed

Nath-Sain S., et al. (2009) LKB1 catalytic activity contributes to estrogen receptor alpha signaling. Mol. Biol. Cell, 20, 2785–2795. PubMed PMC

Gurumurthy S., et al. (2008) LKB1 deficiency sensitizes mice to carcinogen-induced tumorigenesis. Cancer Res., 68, 55–63. PubMed PMC

Ratovitski E.A. (2010) LKB1/PEA3/ΔNp63 pathway regulates PTGS-2 (COX-2) transcription in lung cancer cells upon cigarette smoke exposure. Oxid. Med. Cell. Longev., 3, 317–324. PubMed PMC

Pfeifer G.P., et al. (2002) Tobacco smoke carcinogens, DNA damage and p53 mutations in smoking-associated cancers. Oncogene, 21, 7435–7451. PubMed

Hussain S.P., et al. (2001) Mutability of p53 hotspot codons to benzo(a)pyrene diol epoxide (BPDE) and the frequency of p53 mutations in nontumorous human lung. Cancer Res., 61, 6350–6355. PubMed

Jiang Y., et al. (2007) Ataxia-telangiectasia mutated expression is associated with tobacco smoke exposure in esophageal cancer tissues and benzo[a]pyrene diol epoxide in cell lines. Int. J. Cancer, 120, 91–95. PubMed

Ozturk M. (1991) p53 mutation in hepatocellular carcinoma after aflatoxin exposure. Lancet, 338, 1356–1359. PubMed

Hamid A.S., et al. (2013) Aflatoxin B1-induced hepatocellular carcinoma in developing countries: Geographical distribution, mechanism of action and prevention. Oncol. Lett., 5, 1087–1092. PubMed PMC

Dairkee S.H., et al. (2013) Bisphenol-A-induced inactivation of the p53 axis underlying deregulation of proliferation kinetics, and cell death in non-malignant human breast epithelial cells. Carcinogenesis, 34, 703–712. PubMed PMC

Cohen S.M., et al. (2010) Carcinogenic mode of action of folpet in mice and evaluation of its relevance to humans. Crit. Rev. Toxicol., 40, 531–545. PubMed

Santucci M.A., et al. (2003) Cell-cycle deregulation in BALB/c 3T3 cells transformed by 1,2-dibromoethane and folpet pesticides. Environ. Mol. Mutagen., 41, 315–321. PubMed

Kazantseva Y.A., et al. (2013) Dichlorodiphenyltrichloroethane technical mixture regulates cell cycle and apoptosis genes through the activation of CAR and ERα in mouse livers. Toxicol. Appl. Pharmacol., 271, 137–143. PubMed

Pariseau J., et al. (2009) Potential link between exposure to fungicides chlorothalonil and mancozeb and haemic neoplasia development in the soft-shell clam Mya arenaria: a laboratory experiment. Mar. Pollut. Bull., 58, 503–514. PubMed

Pariseau J., et al. (2011) Effects of pesticide compounds (chlorothalonil and mancozeb) and benzo[a]pyrene mixture on aryl hydrocarbon receptor, p53 and ubiquitin gene expression levels in haemocytes of soft-shell clams (Mya arenaria). Ecotoxicology, 20, 1765–1772. PubMed

Liu Z., et al. (2005) p53 mutations in benzo(a)pyrene-exposed human p53 knock-in murine fibroblasts correlate with p53 mutations in human lung tumors. Cancer Res., 65, 2583–2587. PubMed

Wang J.Y., et al. (1994) The retinoblastoma tumor suppressor protein. Adv. Cancer Res., 64, 25–85. PubMed

Brown M., et al. (1991) Fidelity of mitotic chromosome transmission. Cold Spring Harb. Symp. Quant. Biol., 56, 359–365. PubMed

Weinberg R.A. (1995) The retinoblastoma protein and cell cycle control. Cell, 81, 323–330. PubMed

Weintraub S.J., et al. (1995) Mechanism of active transcriptional repression by the retinoblastoma protein. Nature, 375, 812–815. PubMed

Lundberg A.S., et al. (1998) Functional inactivation of the retinoblastoma protein requires sequential modification by at least two distinct cyclin-cdk complexes. Mol. Cell. Biol., 18, 753–761. PubMed PMC

Kiyokawa H., et al. (1994) Suppression of cyclin-dependent kinase 4 during induced differentiation of erythroleukemia cells. Mol. Cell. Biol., 14, 7195–7203. PubMed PMC

An H.X., et al. (1999) Gene amplification and overexpression of CDK4 in sporadic breast carcinomas is associated with high tumor cell proliferation. Am. J. Pathol., 154, 113–118. PubMed PMC

Papp T., et al. (1999) Mutational analysis of the N-ras, p53, p16INK4a, CDK4, and MC1R genes in human congenital melanocytic naevi. J. Med. Genet., 36, 610–614. PubMed PMC

Konishi N., et al. (2002) Heterogeneous methylation and deletion patterns of the INK4a/ARF locus within prostate carcinomas. Am. J. Pathol., 160, 1207–1214. PubMed PMC

Nielsen G.P., et al. (1998) CDKN2A gene deletions and loss of p16 expression occur in osteosarcomas that lack RB alterations. Am. J. Pathol., 153, 159–163. PubMed PMC

Myong N.H. (2008) Cyclin D1 overexpression, p16 loss, and pRb inactivation play a key role in pulmonary carcinogenesis and have a prognostic implication for the long-term survival in non-small cell lung carcinoma patients. Cancer Res. Treat., 40, 45–52. PubMed PMC

Pietruszewska W., et al. (2008) Loss of heterozygosity for Rb locus and pRb immunostaining in laryngeal cancer: a clinicopathologic, molecular and immunohistochemical study. Folia Histochem. Cytobiol., 46, 479–485. PubMed

Heck J.E., et al. (2013) Retinoblastoma and ambient exposure to air toxics in the perinatal period. J. Expo. Sci. Environ. Epidemiol, 25, 182–186. PubMed PMC

Wiseman R.W., et al. (1994) Allelotyping of butadiene-induced lung and mammary adenocarcinomas of B6C3F1 mice: frequent losses of heterozygosity in regions homologous to human tumor-suppressor genes. Proc. Natl. Acad. Sci. USA, 91, 3759–3763. PubMed PMC

Jeong J.B., et al. (2010) 2-Methoxy-4-vinylphenol can induce cell cycle arrest by blocking the hyper-phosphorylation of retinoblastoma protein in benzo[a]pyrene-treated NIH3T3 cells. Biochem. Biophys. Res. Commun., 400, 752–757. PubMed

Bastide K., et al. (2009) Molecular analysis of the Ink4a/Rb1-Arf/Tp53 pathways in radon-induced rat lung tumors. Lung Cancer, 63, 348–353. PubMed

Torres-Durán M., et al. (2014) Residential radon and lung cancer in never smokers. A systematic review. Cancer Lett., 345, 21–26. PubMed

Li Y., et al. (2011) Up-regulation of cyclin D1 by JNK1/c-Jun is involved in tumorigenesis of human embryo lung fibroblast cells induced by a low concentration of arsenite. Toxicol. Lett., 206, 113–120. PubMed

Ikushima H., et al. (2010) TGFbeta signalling: a complex web in cancer progression. Nat. Rev. Cancer, 10, 415–424. PubMed

Massagué J. (2012) TGFβ signalling in context. Nat. Rev. Mol. Cell Biol., 13, 616–630. PubMed PMC

Lasfar A., et al. (2010) Resistance to transforming growth factor β-mediated tumor suppression in melanoma: are multiple mechanisms in place? Carcinogenesis, 31, 1710–1717. PubMed PMC

Matsuzaki K. (2011) Smad phosphoisoform signaling specificity: the right place at the right time. Carcinogenesis, 32, 1578–1588. PubMed PMC

Yang S., et al. (2008) EGF antagonizes TGF-beta-induced tropoelastin expression in lung fibroblasts via stabilization of Smad corepressor TGIF. Am. J. Physiol. Lung Cell. Mol. Physiol., 295, L143–L151. PubMed PMC

Lo R.S., et al. (2001) Epidermal growth factor signaling via Ras controls the Smad transcriptional co-repressor TGIF. EMBO J., 20, 128–136. PubMed PMC

Dai C., et al. (2004) Hepatocyte growth factor antagonizes the profibrotic action of TGF-beta1 in mesangial cells by stabilizing Smad transcriptional corepressor TGIF. J. Am. Soc. Nephrol., 15, 1402–1412. PubMed

Tan R., et al. (2007) Molecular basis for the cell type specific induction of SnoN expression by hepatocyte growth factor. J. Am. Soc. Nephrol., 18, 2340–2349. PubMed

Kuang C., et al. (2006) In vivo disruption of TGF-beta signaling by Smad7 leads to premalignant ductal lesions in the pancreas. Proc. Natl. Acad. Sci. U. S. A., 103, 1858–1863. PubMed PMC

Luwor R.B., et al. (2013) Targeting Stat3 and Smad7 to restore TGF-β cytostatic regulation of tumor cells in vitro and in vivo . Oncogene, 32, 2433–2441. PubMed PMC

Chi X.Z., et al. (2005) RUNX3 suppresses gastric epithelial cell growth by inducing p21(WAF1/Cip1) expression in cooperation with transforming growth factor {beta}-activated SMAD. Mol. Cell. Biol., 25, 8097–8107. PubMed PMC

Yano T., et al. (2006) The RUNX3 tumor suppressor upregulates Bim in gastric epithelial cells undergoing transforming growth factor beta-induced apoptosis. Mol. Cell. Biol., 26, 4474–4488. PubMed PMC

Ito K., et al. (2011) Loss of Runx3 is a key event in inducing precancerous state of the stomach. Gastroenterology, 140, 1536–46.e8. PubMed

Goh Y.M., et al. (2010) Src kinase phosphorylates RUNX3 at tyrosine residues and localizes the protein in the cytoplasm. J. Biol. Chem., 285, 10122–10129. PubMed PMC

Seoane J., et al. (2004) Integration of Smad and forkhead pathways in the control of neuroepithelial and glioblastoma cell proliferation. Cell, 117, 211–223. PubMed

Gomis R.R., et al. (2006) C/EBPbeta at the core of the TGFbeta cytostatic response and its evasion in metastatic breast cancer cells. Cancer Cell, 10, 203–214. PubMed

Brunet A., et al. (1999) Akt promotes cell survival by phosphorylating and inhibiting a Forkhead transcription factor. Cell, 96, 857–868. PubMed

Azar R., et al. (2009) 4E-BP1 is a target of Smad4 essential for TGFbeta-mediated inhibition of cell proliferation. EMBO J., 28, 3514–3522. PubMed PMC

Bailey K.A., et al. (2012) Transcriptional Modulation of the ERK1/2 MAPK and NF-κB Pathways in Human Urothelial Cells After Trivalent Arsenical Exposure: Implications for Urinary Bladder Cancer. J. Can. Res. Updates, 1, 57–68. PubMed PMC

Germolec D.R., et al. (1996) Arsenic induces overexpression of growth factors in human keratinocytes. Toxicol. Appl. Pharmacol., 141, 308–318. PubMed

Allison P., et al. (2013) Disruption of canonical TGFβ-signaling in murine coronary progenitor cells by low level arsenic. Toxicol. Appl. Pharmacol., 272, 147–153. PubMed PMC

Goodenough D.A., et al. (1996) Connexins, connexons, and intercellular communication. Annu. Rev. Biochem., 65, 475–502. PubMed

Laird D.W. (2006) Life cycle of connexins in health and disease. Biochem. J., 394, 527–543. PubMed PMC

Cronier L., et al. (2009) Gap junctions and cancer: new functions for an old story. Antioxid. Redox Signal., 11, 323–338. PubMed

Naus C.C., et al. (2010) Implications and challenges of connexin connections to cancer. Nat. Rev. Cancer, 10, 435–441. PubMed

Loewenstein W.R., et al. (1967) Intercellular communication and tissue growth. I. Cancerous growth. J. Cell Biol., 33, 225–234. PubMed PMC

Rose B., et al. (1993) Gap-junction protein gene suppresses tumorigenicity. Carcinogenesis, 14, 1073–1075. PubMed

Naus C.C., et al. (1992) In vivo growth of C6 glioma cells transfected with connexin43 cDNA. Cancer Res., 52, 4208–4213. PubMed

Zhu D., et al. (1991) Transfection of C6 glioma cells with connexin 43 cDNA: analysis of expression, intercellular coupling, and cell proliferation. Proc. Natl. Acad. Sci. USA, 88, 1883–1887. PubMed PMC

Leithe E., et al. (2006) Downregulation of gap junctions in cancer cells. Crit. Rev. Oncog., 12, 225–256. PubMed

Mesnil M. (2002) Connexins and cancer. Biol. Cell, 94, 493–500. PubMed

Yamasaki H., et al. (1999) Connexins in tumour suppression and cancer therapy. Novartis Found. Symp., 219, 241–254. PubMed

Moennikes O., et al. (1999) The effect of connexin32 null mutation on hepatocarcinogenesis in different mouse strains. Carcinogenesis, 20, 1379–1382. PubMed

King T.J., et al. (2004) The gap junction protein connexin32 is a mouse lung tumor suppressor. Cancer Res., 64, 7191–7196. PubMed

King T.J., et al. (2004) Mice deficient for the gap junction protein Connexin32 exhibit increased radiation-induced tumorigenesis associated with elevated mitogen-activated protein kinase (p44/Erk1, p42/Erk2) activation. Carcinogenesis, 25, 669–680. PubMed

Plante I., et al. (2011) Cx43 suppresses mammary tumor metastasis to the lung in a Cx43 mutant mouse model of human disease. Oncogene, 30, 1681–1692. PubMed

McLachlan E., et al. (2006) Connexins act as tumor suppressors in three-dimensional mammary cell organoids by regulating differentiation and angiogenesis. Cancer Res., 66, 9886–9894. PubMed

Evans W.H., et al. (2006) The gap junction cellular internet: connexin hemichannels enter the signalling limelight. Biochem. J., 397, 1–14. PubMed PMC

Kandouz M., et al. (2010) Gap junctions and connexins as therapeutic targets in cancer. Expert Opin. Ther. Targets, 14, 681–692. PubMed

Decrock E., et al. (2009) Connexin 43 hemichannels contribute to the propagation of apoptotic cell death in a rat C6 glioma cell model. Cell Death Differ., 16, 151–163. PubMed

Vinken M., et al. (2006) Connexins and their channels in cell growth and cell death. Cell. Signal., 18, 592–600. PubMed

Ito A., et al. (2000) A role for heterologous gap junctions between melanoma and endothelial cells in metastasis. J. Clin. Invest., 105, 1189–1197. PubMed PMC

Stoletov K., et al. (2013) Role of connexins in metastatic breast cancer and melanoma brain colonization. J. Cell Sci., 126(Pt 4), 904–913. PubMed PMC

Sin W.C., et al. (2012) Opposing roles of connexin43 in glioma progression. Biochim. Biophys. Acta, 1818, 2058–2067. PubMed

Duffy H.S., et al. (2006) Cardiac connexins: genes to nexus. Adv. Cardiol., 42, 1–17. PubMed

Meyer R.A., et al. (1992) Inhibition of gap junction and adherens junction assembly by connexin and A-CAM antibodies. J. Cell Biol., 119, 179–189. PubMed PMC

Wei C.J., et al. (2005) Connexin43 associated with an N-cadherin-containing multiprotein complex is required for gap junction formation in NIH3T3 cells. J. Biol. Chem., 280, 19925–19936. PubMed

Matsuuchi L., et al. (2012) Gap junction proteins on the move: connexins, the cytoskeleton and migration. Biochim. Biophys. Acta, 1828, 94–108. PubMed

Ruch R.J., et al. (2001) Gap-junction communication in chemical carcinogenesis. Drug Metab. Rev., 33, 117–124. PubMed

Yamasaki H. (1996) Role of disrupted gap junctional intercellular communication in detection and characterization of carcinogens. Mutat. Res., 365, 91–105. PubMed

Rosenkranz H.S., et al. (2000) Exploring the relationship between the inhibition of gap junctional intercellular communication and other biological phenomena. Carcinogenesis, 21, 1007–1011. PubMed

Bager Y., et al. (1997) Altered function, localization and phosphorylation of gap junctions in rat liver epithelial, IAR 20, cells after treatment with PCBs or TCDD. Environ. Toxicol. Pharmacol., 3, 257–266. PubMed

Hemming H., et al. (1991) Inhibition of dye transfer in rat liver WB cell culture by polychlorinated biphenyls. Pharmacol. Toxicol., 69, 416–420. PubMed

Kang K.S., et al. (1996) Inhibition of gap junctional intercellular communication in normal human breast epithelial cells after treatment with pesticides, PCBs, and PBBs, alone or in mixtures. Environ. Health Perspect., 104, 192–200. PubMed PMC

Ruch R.J., et al. (1986) Effects of tumor promoters, genotoxic carcinogens and hepatocytotoxins on mouse hepatocyte intercellular communication. Cell Biol. Toxicol., 2, 469–483. PubMed

Swierenga S.H., et al. (1990) Effects on intercellular communication in human keratinocytes and liver-derived cells of polychlorinated biphenyl congeners with differing in vivo promotion activities. Carcinogenesis, 11, 921–926. PubMed

Vinken M., et al. (2009) Gap junctional intercellular communication as a target for liver toxicity and carcinogenicity. Crit. Rev. Biochem. Mol. Biol., 44, 201–222. PubMed

Rivedal E., et al. (2003) Supplemental role of the Ames mutation assay and gap junction intercellular communication in studies of possible carcinogenic compounds from diesel exhaust particles. Arch. Toxicol., 77, 533–542. PubMed

Krutovskikh V.A., et al. (1995) Inhibition of rat liver gap junction intercellular communication by tumor-promoting agents in vivo. Association with aberrant localization of connexin proteins. Lab. Invest., 72, 571–577. PubMed

Rutten A.A., et al. (1988) Effect of retinol and cigarette-smoke condensate on dye-coupled intercellular communication between hamster tracheal epithelial cells. Carcinogenesis, 9, 315–320. PubMed

Roemer E., et al. (2013) Characterization of a gap-junctional intercellular communication (GJIC) assay using cigarette smoke. Toxicol. Lett. PubMed

Baker T.K., et al. (1995) Inhibition of gap junctional intercellular communication by 2,3,7,8-tetrachlorodibenzo-p-dioxin (TCDD) in rat hepatocytes. Carcinogenesis, 16, 2321–2326. PubMed

Herrmann S., et al. (2002) Indolo[3,2-b]carbazole inhibits gap junctional intercellular communication in rat primary hepatocytes and acts as a potential tumor promoter. Carcinogenesis, 23, 1861–1868. PubMed

Mally A., et al. (2002) Non-genotoxic carcinogens: early effects on gap junctions, cell proliferation and apoptosis in the rat. Toxicology, 180, 233–248. PubMed

Plante I., et al. (2002) Decreased gap junctional intercellular communication in hexachlorobenzene-induced gender-specific hepatic tumor formation in the rat. Carcinogenesis, 23, 1243–1249. PubMed

De Maio A., et al. (2000) Interruption of hepatic gap junctional communication in the rat during inflammation induced by bacterial lipopolysaccharide. Shock, 14, 53–59. PubMed

Cowles C., et al. (2007) Different mechanisms of modulation of gap junction communication by non-genotoxic carcinogens in rat liver in vivo . Toxicology, 238, 49–59. PubMed

Jeong S.H., et al. (2000) Cadmium decreases gap junctional intercellular communication in mouse liver. Toxicol. Sci., 57, 156–166. PubMed

Gagliano N., et al. (2006) Early cytotoxic effects of ochratoxin A in rat liver: a morphological, biochemical and molecular study. Toxicology, 225, 214–224. PubMed

Ren P., et al. (1998) Inhibition of gap junctional intercellular communication by tumor promoters in connexin43 and connexin32-expressing liver cells: cell specificity and role of protein kinase C. Carcinogenesis, 19, 169–175. PubMed

Horvath A., et al. (2002) Determination of the epigenetic effects of ochratoxin in a human kidney and a rat liver epithelial cell line. Toxicon, 40, 273–282. PubMed

Upham B.L., et al. (2008) Tumor promoting properties of a cigarette smoke prevalent polycyclic aromatic hydrocarbon as indicated by the inhibition of gap junctional intercellular communication via phosphatidylcholine-specific phospholipase C. Cancer Sci., 99, 696–705. PubMed PMC

Upham B.L., et al. (2009) Structure-activity-dependent regulation of cell communication by perfluorinated fatty acids using in vivo and in vitro model systems. Environ. Health Perspect., 117, 545–551. PubMed PMC

Machala M., et al. (2003) Inhibition of gap junctional intercellular communication by noncoplanar polychlorinated biphenyls: inhibitory potencies and screening for potential mode(s) of action. Toxicol. Sci., 76, 102–111. PubMed

Matesic D.F., et al. (1994) Changes in gap-junction permeability, phosphorylation, and number mediated by phorbol ester and non-phorbol-ester tumor promoters in rat liver epithelial cells. Mol. Carcinog., 10, 226–236. PubMed

Leithe E., et al. (2004) Ubiquitination and down-regulation of gap junction protein connexin-43 in response to 12-O-tetradecanoylphorbol 13-acetate treatment. J. Biol. Chem., 279, 50089–50096. PubMed

Rivedal E., et al. (2005) Connexin43 synthesis, phosphorylation, and degradation in regulation of transient inhibition of gap junction intercellular communication by the phorbol ester TPA in rat liver epithelial cells. Exp. Cell Res., 302, 143–152. PubMed

Guan X., et al. (1996) Gap junction endocytosis and lysosomal degradation of connexin43-P2 in WB-F344 rat liver epithelial cells treated with DDT and lindane. Carcinogenesis, 17, 1791–1798. PubMed

Šimečková P, Vondráček J, Andrysík Z, et al. The 2,2’,4,4’,5,5’-hexachlorobiphenyl-enhanced degradation of connexin 43 involves both proteasomal and lysosomal activities. Toxicol Sci 2009; 107: 9–18. PubMed

Gakhar G., et al. (2009) Regulation of gap junctional intercellular communication by TCDD in HMEC and MCF-7 breast cancer cells. Toxicol. Appl. Pharmacol., 235, 171–181. PubMed

Sai K., et al. (1998) Inhibitory effect of pentachlorophenol on gap junctional intercellular communication in rat liver epithelial cells in vitro . Cancer Lett., 130, 9–17. PubMed

Polyak K., et al. (1994) p27Kip1, a cyclin-Cdk inhibitor, links transforming growth factor-beta and contact inhibition to cell cycle arrest. Genes Dev., 8, 9–22. PubMed

Hanahan D., et al. (2011) Hallmarks of cancer: the next generation. Cell, 144, 646–674. PubMed

Lieberman M.A., et al. (1981) Density-dependent regulation of cell growth: an example of a cell-cell recognition phenomenon. J. Membr. Biol., 63, 1–11. PubMed

Halbleib J.M., et al. (2006) Cadherins in development: cell adhesion, sorting, and tissue morphogenesis. Genes Dev., 20, 3199–3214. PubMed

Dietrich C., et al. (1997) Differences in the mechanisms of growth control in contact-inhibited and serum-deprived human fibroblasts. Oncogene, 15, 2743–2747. PubMed

Kato A., et al. (1997) Inactivation of the cyclin D-dependent kinase in the rat fibroblast cell line, 3Y1, induced by contact inhibition. J. Biol. Chem., 272, 8065–8070. PubMed

Levenberg S., et al. (1999) p27 is involved in N-cadherin-mediated contact inhibition of cell growth and S-phase entry. Oncogene, 18, 869–876. PubMed

Deffie A., et al. (1995) Cyclin E restores p53 activity in contact-inhibited cells. Mol. Cell. Biol., 15, 3926–3933. PubMed PMC

Swat A., et al. (2009) Cell density-dependent inhibition of epidermal growth factor receptor signaling by p38alpha mitogen-activated protein kinase via Sprouty2 downregulation. Mol. Cell. Biol., 29, 3332–3343. PubMed PMC

Ewen M.E., et al. (1993) TGF beta inhibition of Cdk4 synthesis is linked to cell cycle arrest. Cell, 74, 1009–1020. PubMed

Grazia Lampugnani M., et al. (2003) Contact inhibition of VEGF-induced proliferation requires vascular endothelial cadherin, beta-catenin, and the phosphatase DEP-1/CD148. J. Cell Biol., 161, 793–804. PubMed PMC

Wang C.Z., et al. (2009) DDR1/E-cadherin complex regulates the activation of DDR1 and cell spreading. Am. J. Physiol. Cell Physiol., 297, C419–C429. PubMed

Shen Y., et al. (2007) SRC utilizes Cas to block gap junctional communication mediated by connexin43. J. Biol. Chem., 282, 18914–18921. PubMed

Alexander D.B., et al. (2004) Normal cells control the growth of neighboring transformed cells independent of gap junctional communication and SRC activity. Cancer Res., 64, 1347–1358. PubMed

Rubin H. (2008) Contact interactions between cells that suppress neoplastic development: can they also explain metastatic dormancy? Adv. Cancer Res., 100, 159–202. PubMed

Li X., et al. (2009) Regulation of miRNA expression by Src and contact normalization: effects on nonanchored cell growth and migration. Oncogene, 28, 4272–4283. PubMed

Jhon Alberto Ochoa-Alvarez CG, et al. (2011) Goldberg contact normalization: mechanisms and pathways to biomarkers and chemotherapeutic targets. In Extracellular and intracellular signaling. RSC Publishing, pp. 105–115.

Panse J., et al. (1997) Fibroblasts transformed by chemical carcinogens are sensitive to intercellular induction of apoptosis: implications for the control of oncogenesis. Carcinogenesis, 18, 259–264. PubMed

Krishnan H., et al. (2012) SRC points the way to biomarkers and chemotherapeutic targets. Genes Cancer, 3, 426–435. PubMed PMC

Oesch F., et al. (1988) 12-O-tetradecanoylphorbol-13-acetate releases human diploid fibroblasts from contact-dependent inhibition of growth. Carcinogenesis, 9, 1319–1322. PubMed

Dietrich C., et al. (2010) The aryl hydrocarbon receptor (AhR) in the regulation of cell-cell contact and tumor growth. Carcinogenesis, 31, 1319–1328. PubMed PMC

Barouki R., et al. (2007) The aryl hydrocarbon receptor, more than a xenobiotic-interacting protein. FEBS Lett., 581, 3608–3615. PubMed

Kung T., et al. (2009) The aryl hydrocarbon receptor (AhR) pathway as a regulatory pathway for cell adhesion and matrix metabolism. Biochem. Pharmacol., 77, 536–546. PubMed PMC

Andrysík Z., et al. (2007) The aryl hydrocarbon receptor-dependent deregulation of cell cycle control induced by polycyclic aromatic hydrocarbons in rat liver epithelial cells. Mutat. Res., 615, 87–97. PubMed

Weiss C., et al. (2008) TCDD deregulates contact inhibition in rat liver oval cells via Ah receptor, JunD and cyclin A. Oncogene, 27, 2198–2207. PubMed

Andrysík Z., et al. (2013) Aryl hydrocarbon receptor-mediated disruption of contact inhibition is associated with connexin43 downregulation and inhibition of gap junctional intercellular communication. Arch. Toxicol., 87, 491–503. PubMed

Andersson H., et al. (2012) Proangiogenic effects of environmentally relevant levels of bisphenol A in human primary endothelial cells. Arch. Toxicol., 86, 465–474. PubMed

Li M.W., et al. (2010) Connexin 43 is critical to maintain the homeostasis of the blood-testis barrier via its effects on tight junction reassembly. Proc. Natl. Acad. Sci. U. S. A., 107, 17998–18003. PubMed PMC

Lin Z.X., et al. (1986) Inhibition of gap junctional intercellular communication in human teratocarcinoma cells by organochlorine pesticides. Toxicol. Appl. Pharmacol., 83, 10–19. PubMed

Ruch R.J., et al. (1987) Inhibition of intercellular communication between mouse hepatocytes by tumor promoters. Toxicol. Appl. Pharmacol., 87, 111–120. PubMed

Liu J., et al. (2015) Tumor suppressor p53 and its mutants in cancer metabolism. Cancer Lett., 356, 197–203. PubMed PMC

Ravi R., et al. (2000) Regulation of tumor angiogenesis by p53-induced degradation of hypoxia-inducible factor 1alpha. Genes Dev., 14, 34–44. PubMed PMC

Hanel W., et al. (2012) Links between mutant p53 and genomic instability. J. Cell. Biochem., 113, 433–439. PubMed PMC

Hacke K., et al. (2010) Regulation of MCP-1 chemokine transcription by p53. Mol. Cancer, 9, 82. PubMed PMC

Tang X., et al. (2012) p53 is an important regulator of CCL2 gene expression. Curr. Mol. Med., 12, 929–943. PubMed PMC

Wang L., et al. (2011) PI3K pathway activation results in low efficacy of both trastuzumab and lapatinib. BMC Cancer, 11, 248. PubMed PMC

Chipuk J.E., et al. (2006) Dissecting p53-dependent apoptosis. Cell Death Differ., 13, 994–1002. PubMed

Nicolay B.N., et al. (2013) Loss of RBF1 changes glutamine catabolism. Genes Dev., 27, 182–196. PubMed PMC

Gabellini C., et al. (2006) Involvement of RB gene family in tumor angiogenesis. Oncogene, 25, 5326–5332. PubMed

Amato A., et al. (2009) CENPA overexpression promotes genome instability in pRb-depleted human cells. Mol. Cancer, 8, 119. PubMed PMC

Attardi L.D., et al. (2013) RB goes mitochondrial. Genes Dev., 27, 975–979. PubMed PMC

Guido C., et al. (2012) Metabolic reprogramming of cancer-associated fibroblasts by TGF-β drives tumor growth: connecting TGF-β signaling with “Warburg-like” cancer metabolism and L-lactate production. Cell Cycle, 11, 3019–3035. PubMed PMC

Geng L., et al. (2013) TGF-beta suppresses VEGFA-mediated angiogenesis in colon cancer metastasis. PLoS One, 8, e59918. PubMed PMC

Glick A.B., et al. (1996) Transforming growth factor beta 1 suppresses genomic instability independent of a G1 arrest, p53, and Rb. Cancer Res., 56, 3645–3650. PubMed

Rao C.V., et al. (2013) Genomic instability and colon carcinogenesis: from the perspective of genes. Front. Oncol., 3, 130. PubMed PMC

Taylor M.A., et al. (2011) Role of TGF-β and the tumor microenvironment during mammary tumorigenesis. Gene Expr., 15, 117–132. PubMed PMC

Mishra S., et al. (2013) Androgen receptor and microRNA-21 axis downregulates transforming growth factor beta receptor II (TGFBR2) expression in prostate cancer. Oncogene. PubMed PMC

Shackelford D.B. (2013) Unravelling the connection between metabolism and tumorigenesis through studies of the liver kinase B1 tumour suppressor. J. Carcinog., 12, 16. PubMed PMC

Londesborough A., et al. (2008) LKB1 in endothelial cells is required for angiogenesis and TGFbeta-mediated vascular smooth muscle cell recruitment. Development, 135, 2331–2338. PubMed

Forcet C., et al. (2007) Dialogue between LKB1 and AMPK: a hot topic at the cellular pole. Sci. STKE, 2007, pe51. PubMed

Gurumurthy S., et al. (2010) The Lkb1 metabolic sensor maintains haematopoietic stem cell survival. Nature, 468, 659–663. PubMed PMC

Takeda S., et al. (2007) LKB1 is crucial for TRAIL-mediated apoptosis induction in osteosarcoma. Anticancer Res., 27, 761–768. PubMed

Gatenby R.A., et al. (2003) The glycolytic phenotype in carcinogenesis and tumor invasion: insights through mathematical models. Cancer Res., 63, 3847–3854. PubMed

Zhu W., et al. (1997) Increased genetic stability of HeLa cells after connexin 43 gene transfection. Cancer Res., 57, 2148–2150. PubMed

Fiaschi T., et al. (2012) Reciprocal metabolic reprogramming through lactate shuttle coordinately influences tumor-stroma interplay. Cancer Res., 72, 5130–5140. PubMed

Gregory S.H., et al. (1979) Glycolytic enzyme activities in malignant cells grown in vitro and in vivo . Cancer Lett., 7, 319–324. PubMed

Feyler S., et al. (2012) Tumour cell generation of inducible regulatory T-cells in multiple myeloma is contact-dependent and antigen-presenting cell-independent. PLoS One, 7, e35981. PubMed PMC

González-Suárez E., et al. (2002) Cooperation between p53 mutation and high telomerase transgenic expression in spontaneous cancer development. Mol. Cell. Biol., 22, 7291–7301. PubMed PMC

Li H., et al. (1999) Molecular interactions between telomerase and the tumor suppressor protein p53 in vitro . Oncogene, 18, 6785–6794. PubMed

Maniwa Y., et al. (2001) Association of p53 gene mutation and telomerase activity in resectable non-small cell lung cancer. Chest, 120, 589–594. PubMed

Lee J.S., et al. (2014) A novel tumor-promoting role for nuclear factor IA in glioblastomas is mediated through negative regulation of p53, p21, and PAI1. Neuro. Oncol., 16, 191–203. PubMed PMC

Goh A.M., et al. (2011) The role of mutant p53 in human cancer. J. Pathol., 223, 116–126. PubMed

Cooks T., et al. (2013) Mutant p53 prolongs NF-κB activation and promotes chronic inflammation and inflammation-associated colorectal cancer. Cancer Cell, 23, 634–646. PubMed PMC

Lorin S., et al. (2013) Autophagy regulation and its role in cancer. Semin. Cancer Biol., 23, 361–379. PubMed

Rayess H., et al. (2012) Cellular senescence and tumor suppressor gene p16. Int. J. Cancer, 130, 1715–1725. PubMed PMC

Sperka T., et al. (2012) DNA damage checkpoints in stem cells, ageing and cancer. Nat. Rev. Mol. Cell Biol., 13, 579–590. PubMed

Gore A.J., et al. (2014) Pancreatic cancer-associated retinoblastoma 1 dysfunction enables TGF-β to promote proliferation. J. Clin. Invest., 124, 338–352. PubMed PMC

Chou N.H., et al. (2006) Expression of altered retinoblastoma protein inversely correlates with tumor invasion in gastric carcinoma. World J. Gastroenterol., 12, 7188–7191. PubMed PMC

Ying L., et al. (2005) Chronic inflammation promotes retinoblastoma protein hyperphosphorylation and E2F1 activation. Cancer Res., 65, 9132–9136. PubMed

Mankame T.P., et al. (2012) The RB tumor suppressor positively regulates transcription of the anti-angiogenic protein NOL7. Neoplasia, 14, 1213–1222. PubMed PMC

Li H., et al. (2006) Transforming growth factor beta suppresses human telomerase reverse transcriptase (hTERT) by Smad3 interactions with c-Myc and the hTERT gene. J. Biol. Chem., 281, 25588–25600. PubMed

Fabregat I., et al. (2013) TGF-beta signaling in cancer treatment. Curr. Pharm. Des, 20, 2934–2947. PubMed

Hasegawa T., et al. (2013) Cancer-associated fibroblasts might sustain the stemness of scirrhous gastric cancer cells via transforming growth factor-β signaling. Int. J. Cancer. PubMed

Bierie B., et al. (2010) Transforming growth factor beta (TGF-beta) and inflammation in cancer. Cytokine Growth Factor Rev., 21, 49–59. PubMed PMC

Bailey JM, Leach SD. (2012) Signaling pathways mediating epithelial- mesenchymal crosstalk in pancreatic cancer: Hedgehog, Notch and TGFbeta. In Grippo PJ, Munshi HG. (eds) Pancreatic cancer and tumor microenvironment. Trivandrum, India. PubMed

Sanchez-Cespedes M. (2011) The role of LKB1 in lung cancer. Fam. Cancer, 10, 447–453. PubMed

Shackelford D.B., et al. (2009) The LKB1-AMPK pathway: metabolism and growth control in tumour suppression. Nat. Rev. Cancer, 9, 563–575. PubMed PMC

Kline E.R., et al. (2013) LKB1 represses focal adhesion kinase (FAK) signaling via a FAK-LKB1 complex to regulate FAK site maturation and directional persistence. J. Biol. Chem., 288, 17663–17674. PubMed PMC

Xu X., et al. (2013) LKB1 controls human bronchial epithelial morphogenesis through p114RhoGEF-dependent RhoA activation. Mol. Cell. Biol., 33, 2671–2682. PubMed PMC

Wingo S.N., et al. (2009) Somatic LKB1 mutations promote cervical cancer progression. PLoS One, 4, e5137. PubMed PMC

Salem A.F., et al. (2012) Two-compartment tumor metabolism: autophagy in the tumor microenvironment and oxidative mitochondrial metabolism (OXPHOS) in cancer cells. Cell Cycle, 11, 2545–2556. PubMed PMC

Spath C., et al. (2013) Inverse relationship between tumor proliferation markers and connexin expression in a malignant cardiac tumor originating from mesenchymal stem cell engineered tissue in a rat in vivo model. Front. Pharmacol., 4, 42. PubMed PMC

Ezumi K., et al. (2008) Aberrant expression of connexin 26 is associated with lung metastasis of colorectal cancer. Clin. Cancer Res., 14, 677–684. PubMed

Ogawa K., et al. (2012) Silencing of connexin 43 suppresses invasion, migration and lung metastasis of rat hepatocellular carcinoma cells. Cancer Sci., 103, 860–867. PubMed PMC

Zhang D., et al. (2012) Cx31.1 acts as a tumour suppressor in non-small cell lung cancer (NSCLC) cell lines through inhibition of cell proliferation and metastasis. J. Cell. Mol. Med., 16, 1047–1059. PubMed PMC

Czyz J. (2008) The stage-specific function of gap junctions during tumourigenesis. Cell. Mol. Biol. Lett., 13, 92–102. PubMed PMC

Corn P.G. (2012) The tumor microenvironment in prostate cancer: elucidating molecular pathways for therapy development. Cancer Manag. Res., 4, 183–193. PubMed PMC

Li J.F., et al. (2014) The effects of cell compressibility, motility and contact inhibition on the growth of tumor cell clusters using the Cellular Potts Model. J. Theor. Biol., 343, 79–91. PubMed PMC

Dixon J.S. (1987) Short-term clinical trials of anti-rheumatoid drugs–an opinion. Agents Actions, 21, 89–92. PubMed

Schrader J., et al. (2009) Restoration of contact inhibition in human glioblastoma cell lines after MIF knockdown. BMC Cancer, 9, 464. PubMed PMC

WARBURG O. (1956) On the origin of cancer cells. Science, 123, 309–314. PubMed

Shackelford D.B., et al. (2009) The LKB1-AMPK pathway: metabolism and growth control in tumour suppression. Nat. Rev. Cancer, 9, 563–575. PubMed PMC

Andrade-Vieira R., et al. (2013) Loss of LKB1 expression reduces the latency of ErbB2-mediated mammary gland tumorigenesis, promoting changes in metabolic pathways. PLoS One, 8, e56567. PubMed PMC

Sen N., et al. (2012) p53 and metabolism: old player in a new game. Transcription, 3, 119–123. PubMed PMC

Zhang C., et al. (2013) Tumour-associated mutant p53 drives the Warburg effect. Nat. Commun., 4, 2935. PubMed PMC

Dasgupta B., et al. (2009) AMP-activated protein kinase phosphorylates retinoblastoma protein to control mammalian brain development. Dev. Cell, 16, 256–270. PubMed PMC

Liu Y., et al. (2012) A small-molecule inhibitor of glucose transporter 1 downregulates glycolysis, induces cell-cycle arrest, and inhibits cancer cell growth in vitro and in vivo . Mol. Cancer Ther., 11, 1672–1682. PubMed

Fillon M. (2012) Getting it right: BPA and the difficulty proving environmental cancer risks. J. Natl. Cancer Inst., 104, 652–655. PubMed

Betancourt A.M., et al. (2012) Altered carcinogenesis and proteome in mammary glands of rats after prepubertal exposures to the hormonally active chemicals bisphenol a and genistein. J. Nutr., 142, 1382S–1388S. PubMed PMC

Durando M., et al. (2011) Prenatal exposure to bisphenol A promotes angiogenesis and alters steroid-mediated responses in the mammary glands of cycling rats. J. Steroid Biochem. Mol. Biol., 127, 35–43. PubMed

Ptak A., et al. (2012) Bisphenol A induces leptin receptor expression, creating more binding sites for leptin, and activates the JAK/Stat, MAPK/ERK and PI3K/Akt signalling pathways in human ovarian cancer cell. Toxicol. Lett., 210, 332–337. PubMed

Pupo M., et al. (2012) Bisphenol A induces gene expression changes and proliferative effects through GPER in breast cancer cells and cancer-associated fibroblasts. Environ. Health Perspect., 120, 1177–1182. PubMed PMC

Goodson W.H.3rd et al.(2011) Activation of the mTOR pathway by low levels of xenoestrogens in breast epithelial cells from high-risk women. Carcinogenesis, 32, 1724–1733. PubMed PMC

Allard P., et al. (2010) Bisphenol A impairs the double-strand break repair machinery in the germline and causes chromosome abnormalities. Proc. Natl. Acad. Sci. USA, 107, 20405–20410. PubMed PMC

Ito Y., et al. (2012) Identification of DNA-dependent protein kinase catalytic subunit (DNA-PKcs) as a novel target of bisphenol A. PLoS One, 7, e50481. PubMed PMC

Takahashi A., et al. (2004) Bisphenol A from dental polycarbonate crown upregulates the expression of hTERT. J. Biomed. Mater. Res. B. Appl. Biomater., 71, 214–221. PubMed

Zhu H., et al. (2010) Environmental endocrine disruptors promote invasion and metastasis of SK-N-SH human neuroblastoma cells. Oncol. Rep., 23, 129–139. PubMed

Hassan Z.K., et al. (2012) Bisphenol A induces hepatotoxicity through oxidative stress in rat model. Oxid. Med. Cell. Longev., 2012, 194829. PubMed PMC

Bratton M.R., et al. (2012) The organochlorine o,p’-DDT plays a role in coactivator-mediated MAPK crosstalk in MCF-7 breast cancer cells. Environ. Health Perspect., 120, 1291–1296. PubMed PMC

Yáñez L., et al. (2004) DDT induces DNA damage in blood cells. Studies in vitro and in women chronically exposed to this insecticide. Environ. Res., 94, 18–24. PubMed

Hurd-Brown T., et al. (2013) Effects of DDT and triclosan on tumor-cell binding capacity and cell-surface protein expression of human natural killer cells. J. Appl. Toxicol., 33, 495–502. PubMed PMC

Arce G.T., et al. (2010) Genetic toxicology of folpet and captan. Crit. Rev. Toxicol., 40, 546–574. PubMed

Canal-Raffin M., et al. (2008) Cytotoxicity of folpet fungicide on human bronchial epithelial cells. Toxicology, 249, 160–166. PubMed

Campos-Pereira F.D., et al. (2012) Early cytotoxic and genotoxic effects of atrazine on Wistar rat liver: a morphological, immunohistochemical, biochemical, and molecular study. Ecotoxicol. Environ. Saf., 78, 170–177. PubMed

Pinchuk L.M., et al. (2007) In vitro atrazine exposure affects the phenotypic and functional maturation of dendritic cells. Toxicol. Appl. Pharmacol., 223, 206–217. PubMed PMC

Hou L., et al. (2013) Lifetime pesticide use and telomere shortening among male pesticide applicators in the Agricultural Health Study. Environ. Health Perspect., 121, 919–924. PubMed PMC

Jin X.T., et al. (2014) Dichlorodiphenyltrichloroethane exposure induces the growth of hepatocellular carcinoma via Wnt/β-catenin pathway. Toxicol. Lett., 225, 158–166. PubMed

Han E.H., et al. (2008) o,p’-DDT induces cyclooxygenase-2 gene expression in murine macrophages: Role of AP-1 and CRE promoter elements and PI3-kinase/Akt/MAPK signaling pathways. Toxicol. Appl. Pharmacol., 233, 333–342. PubMed

Gordon E., et al. (2012) Folpet-induced short term cytotoxic and proliferative changes in the mouse duodenum. Toxicol. Mech. Methods, 22, 54–59. PubMed

Albanito L., et al. (2008) G-protein-coupled receptor 30 and estrogen receptor-alpha are involved in the proliferative effects induced by atrazine in ovarian cancer cells. Environ. Health Perspect., 116, 1648–1655. PubMed PMC

Tsuda H., et al. (2005) High susceptibility of human c-Ha-ras proto-oncogene transgenic rats to carcinogenesis: a cancer-prone animal model. Cancer Sci., 96, 309–316. PubMed PMC

Ueda M., et al. (2005) Possible enhancing effects of atrazine on growth of 7,12-dimethylbenz(a) anthracene-induced mammary tumors in ovariectomized Sprague-Dawley rats. Cancer Sci., 96, 19–25. PubMed PMC

Wetzel L.T., et al. (1994) Chronic effects of atrazine on estrus and mammary tumor formation in female Sprague-Dawley and Fischer 344 rats. J. Toxicol. Environ. Health, 43, 169–182. PubMed

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